Canonical Allele Identifier: PA2826565993
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141193
ClinVar RCV Id: RCV000129588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Arg241_Arg244delinsHis
CA000443
NM_001276760.3:c.721_731delinsCA